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Home » Andrx Did Not Investigate Product Deviations, Form 483 Says
Andrx Did Not Investigate Product Deviations, Form 483 Says
May 8, 2006
Andrx did not properly investigate product discrepancies and out-of-specification results, according to observations listed on the Form 483 the FDA issued to the company after the agency’s reinspection of the drugmaker’s plant in March.
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